HGVS | Genome Assembly |
---|---|
NC_000001.11:g.54999168A>G , CM000663.2:g.54999168A>G | GRCh38 |
NC_000001.10:g.55464841A>G , CM000663.1:g.55464841A>G | GRCh37 |
NC_000001.9:g.55237429A>G | NCBI36 |
NG_008965.1:g.5225A>G | |
NG_008965.2:g.5236A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651561.1:c.-19A>G MANE Select | ENSP00000498282.1:n.-19A>G | |
ENST00000371265.4:c.-19A>G | ENSP00000360312.4:n.-19A>G | |
NM_057176.2:c.-19A>G | NP_476517.1:n.-19A>G | |
NM_057176.3:c.-19A>G MANE Select | NP_476517.1:n.-19A>G |